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B I Brown

Showing results (1-10 of 34) with videos related to

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Nursing Outlook|April 1, 1980
Realistic workloads for community health nursesB I Brown
Archives of Internal Medicine|May 1, 1975
Diphenylhydantoin treatmentB I Brown
American Journal of Human Genetics|March 1, 1989
Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage diseaseB I Brown, D H Brown
Biochemical and Biophysical Research Communications|March 16, 1983
Studies of the residual glycogen branching enzyme activity present in human skin fibroblasts from patients with type IV glycogen storage diseaseD H Brown, B I Brown
Biochemical and Biophysical Research Communications|February 16, 1972
The experimental production of glycogen storage in cultured human fibroblastsB I Brown, D H Brown
Clinical Toxicology|January 1, 1976
Clinical management of the phencyclidine psychosisP V Luisada, B I Brown
Biochemistry|March 17, 1970
Studies of lysosomal alpha-glucosidase. II. Kinetics of action of the rat liver enzymeP L Jeffrey, D H Brown, B I Brown
Biochemistry|March 17, 1970
Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage diseaseB I Brown, D H Brown, P L Jeffrey
Archives of Biochemistry and Biophysics|January 30, 1978
The molecular heterogeneity of purified human liver lysosomal alpha-glucosidase (acid alpha-glucosidase)A K Murray, B I Brown, D H Brown
The Journal of Pediatrics|April 1, 1971
Type IV glycogen storage disease: branching enzyme deficiency in skin fibroblasts and possible heterozygote detectionR R Howell, M M Kaback, B I Brown
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Nursing Outlook|April 1, 1980
Realistic workloads for community health nursesB I Brown
Archives of Internal Medicine|May 1, 1975
Diphenylhydantoin treatmentB I Brown
American Journal of Human Genetics|March 1, 1989
Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage diseaseB I Brown, D H Brown
Biochemical and Biophysical Research Communications|March 16, 1983
Studies of the residual glycogen branching enzyme activity present in human skin fibroblasts from patients with type IV glycogen storage diseaseD H Brown, B I Brown
Biochemical and Biophysical Research Communications|February 16, 1972
The experimental production of glycogen storage in cultured human fibroblastsB I Brown, D H Brown
Clinical Toxicology|January 1, 1976
Clinical management of the phencyclidine psychosisP V Luisada, B I Brown
Biochemistry|March 17, 1970
Studies of lysosomal alpha-glucosidase. II. Kinetics of action of the rat liver enzymeP L Jeffrey, D H Brown, B I Brown
Biochemistry|March 17, 1970
Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage diseaseB I Brown, D H Brown, P L Jeffrey
Archives of Biochemistry and Biophysics|January 30, 1978
The molecular heterogeneity of purified human liver lysosomal alpha-glucosidase (acid alpha-glucosidase)A K Murray, B I Brown, D H Brown
The Journal of Pediatrics|April 1, 1971
Type IV glycogen storage disease: branching enzyme deficiency in skin fibroblasts and possible heterozygote detectionR R Howell, M M Kaback, B I Brown
Pageof 4